Allele Registry

Canonical Allele Identifier: PA916072126

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000001105

RCV003934790

ClinVar Variation:

1050

HGVS (amino-acid)	Matching Registered Transcripts
NP_116103.1:p.Ser186Pro	CA114722 NM_032714.3:c.556T>C