Allele Registry

Canonical Allele Identifier: PA101098

Gene: VPS37A HGNC NCBI

ClinVar Allele:

48340

ClinVar RCV:

RCV000032956

ClinVar Variation:

39741

HGVS (amino-acid)	Matching Registered Transcripts
NP_689628.2:p.Lys382Asn	CA213061 NM_152415.3:c.1146A>T CA370405454 NM_152415.3:c.1146A>C