Allele Registry

Canonical Allele Identifier: PA252037

Gene: UNC13D HGNC NCBI

ClinVar RCV:

RCV000002079

ClinVar Variation:

2002

HGVS (amino-acid)	Matching Registered Transcripts
NP_954712.1:p.Leu403Pro	CA252035 NM_199242.3:c.1208T>C