ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645435739
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000229442
RCV000418894
RCV000419610
RCV000420292
RCV000420936
RCV000421633
RCV000424795
RCV000425414
RCV000425773
RCV000426089
RCV000430314
RCV000430964
RCV000431663
RCV000432304
RCV000432999
RCV000434831
RCV000435488
RCV000436124
RCV000436850
RCV000438849
RCV000441018
RCV000441674
RCV000443867
RCV000444130
RCV000444805
RCV000445077
RCV002378977
RCV004020765
ClinVar Variation:
237954
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119586.1:p.Arg248Pro
CA10583676
NM_001126114.3:c.743G>C