Allele Registry

Canonical Allele Identifier: PA267505

Gene: STX11 HGNC NCBI

ClinVar RCV:

RCV000083252

RCV001269565

ClinVar Variation:

97001

HGVS (amino-acid)	Matching Registered Transcripts
NP_003755.2:p.Leu58Pro	CA267503 NM_003764.4:c.173T>C