Canonical Allele Identifier: PA658679473
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro20Ser
CA002580
NM_001126117.1:c.58C>T