Canonical Allele Identifier: PA2825782586
Gene: STX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 339046
ClinVar RCV Id: RCV000262733 RCV004021841
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128244.1:p.Arg69Trp
CA9925244
NM_001134772.3:c.205C>T