Canonical Allele Identifier: PA2580296022
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1903679
ClinVar RCV Id: RCV002573086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Leu41Pro
CA365948579
NM_003764.4:c.122T>C