Canonical Allele Identifier: PA164819
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 80708
ClinVar RCV Id: RCV000129635 RCV000701624 RCV001127281 RCV001358057 RCV003894916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.His326Tyr
CA000035
NM_001126118.1:c.976C>T