Allele Registry

Canonical Allele Identifier: PA658809617

Gene: INF2 HGNC NCBI

ClinVar Variation Id: 540041

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Asp997Asn	CA7373145 NM_022489.4:c.2989G>A