Allele Registry

Canonical Allele Identifier: PA658809584

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000649983

ClinVar Variation:

540057

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Glu719Lys	CA7372850 NM_022489.4:c.2155G>A