Allele Registry

Canonical Allele Identifier: PA658809575

Gene: INF2 HGNC NCBI

ClinVar Variation Id: 498799

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Arg622Gly	CA7372691 NM_022489.4:c.1864C>G