Canonical Allele Identifier: PA2826984843
Gene: SNX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 40050
ClinVar RCV Id: RCV000033149 RCV002514140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305128.1:p.Arg51Gln
CA130726
NM_001318199.3:c.152G>A