Allele Registry

Canonical Allele Identifier: PA2828115382

Gene: VMA21 HGNC NCBI

ClinVar RCV:

RCV000190830

ClinVar Variation:

208802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350739.1:p.Gly146Ala	CA10575764 NM_001363810.1:c.437G>C