Canonical Allele Identifier: PA2830365334
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 160301
ClinVar RCV Id: RCV000147972 RCV000710287 RCV000576791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775907.4:p.Leu1385Phe
CA173941
NM_173636.5:c.4155A>C
CA405460348
NM_173636.5:c.4155A>T