Allele Registry

Canonical Allele Identifier: PA111469

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000001105

RCV003934790

ClinVar Variation:

1050

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Ser186Pro	CA114722 NM_022489.4:c.556T>C