Allele Registry

Canonical Allele Identifier: PA645490242

Gene: INF2 HGNC NCBI

ClinVar Variation Id: 426793

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Thr1179Ala	CA7373296 NM_022489.4:c.3535A>G