Canonical Allele Identifier: PA2826563072
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509915
ClinVar RCV Id: RCV002011381
ClinVar Variation Id: 1521256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Glu21Asp
CA397841280
NM_001276698.3:c.63G>T
CA397841283
NM_001276698.3:c.63G>C