Allele Registry

Canonical Allele Identifier: PA2825350442

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV001254082

RCV002570553

ClinVar Variation:

976701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026884.3:p.Leu78del	CA2160924684 NM_001031714.3:c.232_234del