Canonical Allele Identifier: PA173942
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_001077430.1:p.Leu1390Phe
CA173941
NM_001083961.2:c.4170A>C
CA405460348
NM_001083961.2:c.4170A>T