Allele Registry

Canonical Allele Identifier: PA916072019

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV001378572

ClinVar Variation:

472835

HGVS (amino-acid)	Matching Registered Transcripts
NP_116103.1:p.Val105Glu	CA391225858 NM_032714.3:c.314T>A