Allele Registry

Canonical Allele Identifier: PA2825781924

Gene: NFIA HGNC NCBI

ClinVar RCV:

RCV000484251

ClinVar Variation:

423556

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128145.1:p.Cys103Ser	CA16617175 NM_001134673.4:c.308G>C CA340586747 NM_001134673.4:c.307T>A