Canonical Allele Identifier: PA2825516967
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 1465591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Ser1070Phe
CA9396181
NM_001083961.2:c.3209C>T