Canonical Allele Identifier: PA2825602919
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Ala69Gly
CA10580956
NM_001126113.3:c.206C>G