Canonical Allele Identifier: PA2825516953
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 1336951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Ser1022Leu
CA9396130
NM_001083961.2:c.3065C>T