Canonical Allele Identifier: PA2573217395
Gene: SYT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 30861
ClinVar RCV Id: RCV000023846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001384474.1:p.Gly729Asp
CA129507
NM_001397545.1:c.2186G>A