Canonical Allele Identifier: PA174486
Gene: STX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161626
ClinVar RCV Id: RCV000149162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004844.1:p.Gln145Pro
CA174485
NM_004853.3:c.434A>C