Allele Registry

Canonical Allele Identifier: PA2830292072

Gene: SNX7 HGNC NCBI

ClinVar Variation Id: 719339

HGVS (amino-acid)	Matching Registered Transcripts
NP_689424.2:p.Phe195Leu	CA964085 NM_152238.4:c.585C>A CA341381973 NM_152238.4:c.583T>C CA341381978 NM_152238.4:c.585C>G