Canonical Allele Identifier: PA645436312
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Tyr88Asn
CA16603101
NM_001126117.1:c.262T>A