Canonical Allele Identifier: PA2826488998
Gene: SNX17 HGNC NCBI

Linked Data

ClinVar Variation Id: 2303371
ClinVar RCV Id: RCV004154671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001253988.1:p.Arg261Cys
CA1577436
NM_001267059.2:c.781C>T