Allele Registry

Canonical Allele Identifier: PA2825350634

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000789988

RCV001380434

RCV002462135

RCV004027379

ClinVar Variation:

637706

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026884.3:p.Leu132Pro	CA391212614 NM_001031714.3:c.395T>C