Allele Registry

Canonical Allele Identifier: PA2825352292

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV001342913

ClinVar Variation:

1039439

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026884.3:p.Arg1211Leu	CA7373326 NM_001031714.3:c.3632G>T