Canonical Allele Identifier: PA2826567300
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly206Val
CA001743
NM_001276761.3:c.617G>T
CA645588573
NM_001276761.3:c.617_618delinsTT