Allele Registry

Canonical Allele Identifier: PA111169

Gene: SNX10 HGNC NCBI

ClinVar RCV:

RCV000033149

RCV002514140

ClinVar Variation:

40050

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186764.1:p.Arg51Gln	CA130726 NM_001199835.1:c.152G>A