Allele Registry

Canonical Allele Identifier: PA645405087

Gene: NFIA HGNC NCBI

ClinVar RCV:

RCV000484251

ClinVar Variation:

423556

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138983.1:p.Cys95Ser	CA16617175 NM_001145511.2:c.284G>C CA340586747 NM_001145511.2:c.283T>A