Canonical Allele Identifier: PA2828064469
Gene: SNX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 40050
ClinVar RCV Id: RCV000033149 RCV002514140
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349682.1:p.Arg77Gln
CA130726
NM_001362753.1:c.230G>A