Canonical Allele Identifier: PA2826567835
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186887
ClinVar Variation Id: 1785528
ClinVar RCV Id: RCV002422277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly321Arg
CA000028
NM_001276761.3:c.961G>A
CA397831931
NM_001276761.3:c.961G>C