Allele Registry

Canonical Allele Identifier: PA1139686005

Gene: VMA21 HGNC NCBI

ClinVar Allele:

939463

ClinVar RCV:

RCV001208862

RCV003238319

ClinVar Variation:

939455

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017980.1:p.Ala75Thr	CA415271253 NM_001017980.4:c.223G>A