Allele Registry

Canonical Allele Identifier: PA1139756533

Gene: UNC13D HGNC NCBI

ClinVar Allele:

950300

ClinVar RCV:

RCV001234601

RCV001844275

RCV002264238

ClinVar Variation:

960980

HGVS (amino-acid)	Matching Registered Transcripts
NP_954712.1:p.Ser290Leu	CA8773227 NM_199242.3:c.869C>T