Allele Registry

Canonical Allele Identifier: PA2825350538

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000755018

ClinVar Variation:

617764

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026884.3:p.Cys104Tyr	CA391225853 NM_001031714.3:c.311G>A