ClinGen Allele Registry
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Canonical Allele Identifier:
PA348463
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
219759
ClinVar RCV Id:
RCV000204217
RCV000424345
RCV000424462
RCV000430896
RCV000433956
RCV000432845
RCV000433328
RCV000445176
RCV000418073
RCV000445265
RCV000423238
RCV000425587
RCV000435222
RCV000440475
RCV000441597
RCV000492197
RCV004020511
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119586.1:p.Tyr234Asp
CA348450
NM_001126114.3:c.700T>G