ClinGen Allele Registry
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Canonical Allele Identifier:
PA645435692
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000418366
RCV000419457
RCV000420564
RCV000422775
RCV000423557
RCV000424609
RCV000425684
RCV000426866
RCV000429686
RCV000432077
RCV000434790
RCV000434877
RCV000435947
RCV000437125
RCV000440449
RCV000441702
RCV000441931
RCV000441961
RCV000443160
RCV001045859
RCV002374627
RCV004022242
ClinVar Variation:
376665
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119586.1:p.Ser241Ala
CA16603080
NM_001126114.3:c.721T>G