Canonical Allele Identifier: PA2826565634
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Tyr181Ser
CA000314
NM_001276760.3:c.542A>C