Canonical Allele Identifier: PA2826562626
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024359
ClinVar RCV Id: RCV001324527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ser144Arg
CA397836305
NM_001276697.3:c.432C>G
CA397836307
NM_001276697.3:c.432C>A
CA397836320
NM_001276697.3:c.430A>C