Canonical Allele Identifier: PA2826277722
Gene: STX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 339054
ClinVar RCV Id: RCV000398773 RCV002520025 RCV002520026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191797.1:p.His162Leu
CA9925381
NM_001204868.2:c.485A>T