Canonical Allele Identifier: PA645496636
Gene: WDR36 HGNC NCBI

Linked Data

ClinVar Variation Id: 424172
ClinVar RCV Id: RCV000482086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_644810.1:p.Cys2Tyr
CA16618061
NM_139281.2:c.5G>A