Allele Registry

Canonical Allele Identifier: PA101827

Gene: SYT14 HGNC NCBI

ClinVar RCV:

RCV000023846

ClinVar Variation:

30861

HGVS (amino-acid)	Matching Registered Transcripts
NP_694994.2:p.Gly439Asp	CA129507 NM_153262.5:c.1316G>A