Allele Registry

Canonical Allele Identifier: PA2825882999

Gene: VPS37A HGNC NCBI

ClinVar Allele:

48340

ClinVar RCV:

RCV000032956

ClinVar Variation:

39741

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138624.1:p.Lys357Asn	CA213061 NM_001145152.2:c.1071A>T CA370405454 NM_001145152.2:c.1071A>C