Allele Registry

Canonical Allele Identifier: PA658675552

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000542048

ClinVar Variation:

472842

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Gly73Val	CA267330465 NM_022489.4:c.218G>T