Canonical Allele Identifier: PA2580296025
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2184940
ClinVar RCV Id: RCV002603568 RCV003479480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Lys83Glu
CA4031663
NM_003764.4:c.247A>G