Allele Registry

Canonical Allele Identifier: PA2580130998

Gene: C9orf152 HGNC NCBI

ClinVar RCV:

RCV004238754

ClinVar Variation:

2401868

HGVS (amino-acid)	Matching Registered Transcripts
NP_001013011.2:p.Asn77Ser	CA198307090 NM_001012993.3:c.230A>G