Canonical Allele Identifier: PA645386151
Gene: STX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 391808
ClinVar RCV Id: RCV000435289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443106.1:p.Lys252Ile
CA16607299
NM_052874.4:c.755A>T