Canonical Allele Identifier: PA645479528
Gene: STX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 339054
ClinVar RCV Id: RCV000398773 RCV002520025 RCV002520026
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001433.1:p.His215Leu
CA9925381
NM_001001433.3:c.644A>T