Canonical Allele Identifier: PA2826277698
Gene: STX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 339046
ClinVar RCV Id: RCV000262733 RCV004021841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191797.1:p.Arg20Trp
CA9925244
NM_001204868.2:c.58C>T