Allele Registry

Canonical Allele Identifier: PA645417203

Gene: VMA21 HGNC NCBI

ClinVar RCV:

RCV000190830

ClinVar Variation:

208802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017980.1:p.Gly91Ala	CA10575764 NM_001017980.4:c.272G>C