Allele Registry

Canonical Allele Identifier: PA2825350377

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000534855

ClinVar Variation:

472837

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026884.3:p.Tyr50Asp	CA391225100 NM_001031714.3:c.148T>G