Allele Registry

Canonical Allele Identifier: PA916072013

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000755018

ClinVar Variation:

617764

HGVS (amino-acid)	Matching Registered Transcripts
NP_116103.1:p.Cys104Tyr	CA391225853 NM_032714.3:c.311G>A