Canonical Allele Identifier: PA169618
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Asp57Glu
CA000060
NM_000546.6:c.171C>A
CA397846290
NM_000546.6:c.171C>G