Canonical Allele Identifier: PA194087
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Thr155Ser
CA000210
NM_001126114.3:c.464C>G
CA397842094
NM_001126114.3:c.463A>T