Allele Registry

Canonical Allele Identifier: PA2829607787

Gene: NFIA HGNC NCBI

ClinVar RCV:

RCV000484251

ClinVar Variation:

423556

HGVS (amino-acid)	Matching Registered Transcripts
NP_005586.1:p.Cys103Ser	CA16617175 NM_005595.5:c.308G>C CA340586747 NM_005595.5:c.307T>A