Allele Registry

Canonical Allele Identifier: PA2829285048

Gene: SYT14 HGNC NCBI

ClinVar RCV:

RCV000023846

ClinVar Variation:

30861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001384473.1:p.Gly729Asp	CA129507 NM_001397544.1:c.2186G>A