Allele Registry

Canonical Allele Identifier: PA916072037

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000789988

RCV001380434

RCV002462135

RCV004027379

ClinVar Variation:

637706

HGVS (amino-acid)	Matching Registered Transcripts
NP_116103.1:p.Leu132Pro	CA391212614 NM_032714.3:c.395T>C