Allele Registry

Canonical Allele Identifier: PA2828080859

Gene: VPS37A HGNC NCBI

ClinVar RCV:

RCV000032956

ClinVar Variation:

39741

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350096.1:p.Lys376Asn	CA213061 NM_001363167.1:c.1128A>T CA370405454 NM_001363167.1:c.1128A>C