Canonical Allele Identifier: PA2825619002
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024359
ClinVar RCV Id: RCV001324527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ser264Arg
CA397836305
NM_001126118.1:c.792C>G
CA397836307
NM_001126118.1:c.792C>A
CA397836320
NM_001126118.1:c.790A>C