Canonical Allele Identifier: PA2826489021
Gene: SNX17 HGNC NCBI

Linked Data

ClinVar Variation Id: 2545232
ClinVar RCV Id: RCV004314955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001253989.1:p.Thr240Met
CA44524714
NM_001267060.2:c.719C>T