Canonical Allele Identifier: PA191629
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185319
ClinVar RCV Id: RCV000164718 RCV003765021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ala276Gly
CA000436
NM_000546.6:c.827C>G