Allele Registry

Canonical Allele Identifier: PA2580566457

Gene: UNC13D HGNC NCBI

ClinVar RCV:

RCV002283946

ClinVar Variation:

1705632

HGVS (amino-acid)	Matching Registered Transcripts
NP_954712.1:p.Glu1017Lys	CA8772294 NM_199242.3:c.3049G>A