Canonical Allele Identifier: PA891861860
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 569629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ala39Val
CA397847899
NM_001126114.3:c.116C>T