Canonical Allele Identifier: PA2830365181
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327895
ClinVar RCV Id: RCV001794837 RCV002541278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775907.4:p.Phe1087Leu
CA9396234
NM_173636.5:c.3261C>G
CA405451841
NM_173636.5:c.3259T>C
CA405451856
NM_173636.5:c.3261C>A