Canonical Allele Identifier: PA645436237
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 231661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg70Gly
CA10580933
NM_001126117.1:c.208C>G