Canonical Allele Identifier: PA2573065187
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Phe1092Leu
CA9396234
NM_001083961.2:c.3276C>G
CA405451841
NM_001083961.2:c.3274T>C
CA405451856
NM_001083961.2:c.3276C>A