Canonical Allele Identifier: PA2829472201
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3171721
ClinVar RCV Id: RCV004458592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Ser81Asn
CA365948821
NM_003764.4:c.242G>A