Allele Registry

Canonical Allele Identifier: PA2825352171

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000497978

RCV003766802

ClinVar Variation:

432619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026884.3:p.Ala1165Val	CA7373277 NM_001031714.3:c.3494C>T