Allele Registry

Canonical Allele Identifier: PA658675570

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000546565

RCV002384232

ClinVar Variation:

472870

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Leu245Val	CA7372412 NM_022489.4:c.733C>G