Canonical Allele Identifier: PA2825601828
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024359
ClinVar RCV Id: RCV001324527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ser303Arg
CA397836305
NM_001126112.3:c.909C>G
CA397836307
NM_001126112.3:c.909C>A
CA397836320
NM_001126112.3:c.907A>C