Canonical Allele Identifier: PA2579954970
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016947
ClinVar RCV Id: RCV001316024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ser15Arg
CA397849035
NM_000546.6:c.45T>G
CA397849047
NM_000546.6:c.45T>A
CA397849074
NM_000546.6:c.43A>C