Allele Registry

Canonical Allele Identifier: PA658675618

Gene: INF2 HGNC NCBI

ClinVar Variation Id: 472850

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Arg1045Trp	CA7373186 NM_022489.4:c.3133C>T