Allele Registry

Canonical Allele Identifier: PA915985448

Gene: SYT14 HGNC NCBI

ClinVar RCV:

RCV000023846

ClinVar Variation:

30861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139736.1:p.Gly484Asp	CA129507 NM_001146264.4:c.1451G>A