Canonical Allele Identifier: PA2829285064
Gene: SYT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 448643
ClinVar RCV Id: RCV000518128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001384474.1:p.Ser381Asn
CA344605957
NM_001397545.1:c.1142G>A