Canonical Allele Identifier: PA2826567145
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Tyr181Asn
CA16603101
NM_001276761.3:c.541T>A