Canonical Allele Identifier: PA2579953867
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ala69Gly
CA10580956
NM_000546.6:c.206C>G