Canonical Allele Identifier: PA915976712
Gene: STX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 339043
ClinVar RCV Id: RCV000268540 RCV000971975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128244.1:p.Pro36Thr
CA9925170
NM_001134772.3:c.106C>A