Canonical Allele Identifier: PA294064
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Thr180Ser
CA000505
NM_001126117.1:c.539C>G
CA397836079
NM_001126117.1:c.538A>T