Canonical Allele Identifier: PA2825598493
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 496047
ClinVar Variation Id: 528238
ClinVar RCV Id: RCV000633332
ClinVar Variation Id: 821828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ser9Arg
CA003949
NM_001126112.3:c.27C>G
CA397849245
NM_001126112.3:c.27C>A
CA397849282
NM_001126112.3:c.25A>C