Allele Registry

Canonical Allele Identifier: PA2828196050

Gene: NFIX HGNC NCBI

ClinVar Variation Id: 452926

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352914.1:p.Met47Lys	CA404313335 NM_001365985.2:c.140T>A