Allele Registry

Canonical Allele Identifier: PA658655260

Gene: UNC13D HGNC NCBI

ClinVar RCV:

RCV000514775

RCV001778988

RCV003497856

ClinVar Variation:

445606

HGVS (amino-acid)	Matching Registered Transcripts
NP_954712.1:p.Glu616Gly	CA401092049 NM_199242.3:c.1847A>G