Allele Registry

Canonical Allele Identifier: PA2828081255

Gene: VPS37A HGNC NCBI

ClinVar Allele:

48340

ClinVar RCV:

RCV000032956

ClinVar Variation:

39741

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350100.1:p.Lys286Asn	CA213061 NM_001363171.1:c.858A>T CA370405454 NM_001363171.1:c.858A>C