Allele Registry

Canonical Allele Identifier: PA2826367322

Gene: SYT14 HGNC NCBI

ClinVar RCV:

RCV000023846

ClinVar Variation:

30861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001242935.1:p.Gly401Asp	CA129507 NM_001256006.3:c.1202G>A