Allele Registry

Canonical Allele Identifier: PA2826984758

Gene: SNX10 HGNC NCBI

ClinVar RCV:

RCV000033149

RCV002514140

ClinVar Variation:

40050

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305127.1:p.Arg77Gln	CA130726 NM_001318198.1:c.230G>A