Canonical Allele Identifier: PA2826248771
Gene: SNX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369116
ClinVar RCV Id: RCV001874582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186766.1:p.Gln62Arg
CA367228198
NM_001199837.3:c.185A>G