Allele Registry

Canonical Allele Identifier: PA099955

Gene: IMPG2 HGNC NCBI

ClinVar Variation Id: 3550

HGVS (amino-acid)	Matching Registered Transcripts
NP_057331.2:p.Phe124Leu	CA116343 NM_016247.4:c.370T>C CA353851939 NM_016247.4:c.372T>A CA353851940 NM_016247.4:c.372T>G