Canonical Allele Identifier: PA658665596
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_001139733.1:p.Ser136Asn
CA344605957
NM_001146261.4:c.407G>A