Canonical Allele Identifier: PA2826984766
Gene: SNX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369116
ClinVar RCV Id: RCV001874582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305127.1:p.Gln91Arg
CA367228198
NM_001318198.1:c.272A>G