Canonical Allele Identifier: PA2741945681
Gene: SNX17 HGNC NCBI

Linked Data

ClinVar Variation Id: 2545232
ClinVar RCV Id: RCV004314955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055563.1:p.Thr265Met
CA44524714
NM_014748.3:c.794C>T