Allele Registry

Canonical Allele Identifier: PA111413

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000023853

ClinVar Variation:

30868

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Leu132Arg	CA129513 NM_022489.4:c.395T>G