Canonical Allele Identifier: PA2825928374
Gene: SYT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 448643
ClinVar RCV Id: RCV000518128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139734.1:p.Ser91Asn
CA344605957
NM_001146262.4:c.272G>A