Canonical Allele Identifier: PA1139752389
Gene: STX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 862668
ClinVar RCV Id: RCV001069433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443106.1:p.Arg245Gln
CA395646822
NM_052874.4:c.734G>A