Allele Registry

Canonical Allele Identifier: PA658675615

Gene: INF2 HGNC NCBI

ClinVar Variation Id: 447577

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Thr1027Met	CA7373176 NM_022489.4:c.3080C>T