Canonical Allele Identifier: PA2499295348
Gene: STX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1010415
ClinVar RCV Id: RCV001308036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443106.1:p.Arg231His
CA395646938
NM_052874.4:c.692G>A