Canonical Allele Identifier: PA207618
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 196613
ClinVar RCV Id: RCV000193857 RCV000351552 RCV000714196 RCV002517711
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Ala1271Val
CA207617
NM_001083961.2:c.3812C>T