Canonical Allele Identifier: PA658664708
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458541
ClinVar RCV Id: RCV000547041 RCV000785493 RCV001021115 RCV002289730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Tyr87Cys
CA397843956
NM_001126118.1:c.260A>G