Allele Registry

Canonical Allele Identifier: PA645490242

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000490158

RCV000649970

RCV002455952

ClinVar Variation:

426793

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Thr1179Ala	CA7373296 NM_022489.4:c.3535A>G