Canonical Allele Identifier: PA165052
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141302
ClinVar RCV Id: RCV000129770 RCV000633376 RCV002288629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Phe113Val
CA000124
NM_000546.6:c.337T>G