Allele Registry

Canonical Allele Identifier: PA658675649

Gene: INF2 HGNC NCBI

ClinVar Allele:

463111

ClinVar RCV:

RCV000535958

RCV001112661

ClinVar Variation:

472862

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Pro1235Ser	CA7373370 NM_022489.4:c.3703C>T