Allele Registry

Canonical Allele Identifier: PA2825350631

Gene: INF2 HGNC NCBI

ClinVar Allele:

39825

ClinVar RCV:

RCV000023853

ClinVar Variation:

30868

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026884.3:p.Leu132Arg	CA129513 NM_001031714.3:c.395T>G