Canonical Allele Identifier: PA132778
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 43588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Pro47Ser
CA000053
NM_001126113.3:c.139C>T