Allele Registry

Canonical Allele Identifier: PA2828158441

Gene: SNX7 HGNC NCBI

ClinVar Variation Id: 719339

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351832.1:p.Phe186Leu	CA964085 NM_001364903.1:c.558C>A CA341381973 NM_001364903.1:c.556T>C CA341381978 NM_001364903.1:c.558C>G