Canonical Allele Identifier: PA2825598901
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ala69Gly
CA10580956
NM_001126112.3:c.206C>G