Canonical Allele Identifier: PA2826489022
Gene: SNX17 HGNC NCBI

Linked Data

ClinVar Variation Id: 2303371
ClinVar RCV Id: RCV004154671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001253989.1:p.Arg248Cys
CA1577436
NM_001267060.2:c.742C>T