Allele Registry

Canonical Allele Identifier: PA916072030

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000023853

ClinVar Variation:

30868

HGVS (amino-acid)	Matching Registered Transcripts
NP_116103.1:p.Leu132Arg	CA129513 NM_032714.3:c.395T>G