Canonical Allele Identifier: PA2826488997
Gene: SNX17 HGNC NCBI

Linked Data

ClinVar Variation Id: 2545232
ClinVar RCV Id: RCV004314955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001253988.1:p.Thr253Met
CA44524714
NM_001267059.2:c.758C>T