Canonical Allele Identifier: PA2825517052
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 2274922
ClinVar RCV Id: RCV002817598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.His1422Asp
CA307843108
NM_001083961.2:c.4264C>G