Allele Registry

Canonical Allele Identifier: PA2828081060

Gene: VPS37A HGNC NCBI

ClinVar RCV:

RCV000032956

ClinVar Variation:

39741

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350098.1:p.Lys292Asn	CA213061 NM_001363169.1:c.876A>T CA370405454 NM_001363169.1:c.876A>C