Canonical Allele Identifier: PA2573207725
Gene: SNX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369116
ClinVar RCV Id: RCV001874582
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349683.1:p.Gln91Arg
CA367228198
NM_001362754.1:c.272A>G