Allele Registry

Canonical Allele Identifier: PA658809603

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000649967

RCV002440354

RCV003420140

ClinVar Variation:

540045

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Leu919Val	CA7373055 NM_022489.4:c.2755C>G