Allele Registry

Canonical Allele Identifier: PA252027

Gene: UNC13D HGNC NCBI

ClinVar Allele:

17035

ClinVar RCV:

RCV000002073

ClinVar Variation:

1996

HGVS (amino-acid)	Matching Registered Transcripts
NP_954712.1:p.Arg610_Gln613del	CA252025 NM_199242.3:c.1828_1839del