Canonical Allele Identifier: PA174263
Gene: ZNF717 HGNC NCBI

Linked Data

ClinVar Variation Id: 161523
ClinVar RCV Id: RCV000149058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121695.1:p.Leu410Val
CA174262
NM_001128223.3:c.1228C>G