Canonical Allele Identifier: PA2825598837
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779558
ClinVar RCV Id: RCV002401652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Gly59Ser
CA397846266
NM_001126112.3:c.175G>A