Allele Registry

Canonical Allele Identifier: PA2573075031

Gene: NFIX HGNC NCBI

ClinVar Variation Id: 452926

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365334.1:p.Met64Lys	CA404313335 NM_001378405.1:c.191T>A