Canonical Allele Identifier: PA658679131
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro13Arg
CA397849109
NM_001126114.3:c.38C>G