Allele Registry

Canonical Allele Identifier: PA111324

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000001106

RCV000681691

RCV001239762

RCV002293970

RCV003352745

ClinVar Variation:

1051

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Arg218Gln	CA114723 NM_022489.4:c.653G>A