Allele Registry

Canonical Allele Identifier: PA645489819

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000428001

RCV001221125

ClinVar Variation:

388001

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Arg261Gln	CA7372422 NM_022489.4:c.782G>A