Allele Registry

Canonical Allele Identifier: PA2828189794

Gene: NFIX HGNC NCBI

ClinVar Variation Id: 452926

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352831.1:p.Met48Lys	CA404313335 NM_001365902.3:c.143T>A