Canonical Allele Identifier: PA1139705259
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 964839
ClinVar RCV Id: RCV001239148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Asn55Ser
CA4031640
NM_003764.4:c.164A>G