Allele Registry

Canonical Allele Identifier: PA111446

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000001109

ClinVar Variation:

1054

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Leu42Pro	CA114726 NM_022489.4:c.125T>C