Allele Registry

Canonical Allele Identifier: PA2826248763

Gene: SNX10 HGNC NCBI

ClinVar RCV:

RCV000033149

RCV002514140

ClinVar Variation:

40050

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186766.1:p.Arg48Gln	CA130726 NM_001199837.3:c.143G>A