Allele Registry

Canonical Allele Identifier: PA2829216780

Gene: SMG7 HGNC NCBI

ClinVar Allele:

2222193

ClinVar RCV:

RCV004104943

ClinVar Variation:

2239241

HGVS (amino-acid)	Matching Registered Transcripts
NP_001381073.1:p.Phe255Leu	CA343687753 NM_001394144.1:c.763T>C CA343687759 NM_001394144.1:c.765T>A CA343687762 NM_001394144.1:c.765T>G