Allele Registry

Canonical Allele Identifier: PA2573314822

Gene: UNC13D HGNC NCBI

ClinVar RCV:

RCV001933527

ClinVar Variation:

1427006

HGVS (amino-acid)	Matching Registered Transcripts
NP_954712.1:p.Arg256Gly	CA8773278 NM_199242.3:c.766C>G