Canonical Allele Identifier: PA2826531635
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 2500469
ClinVar RCV Id: RCV003225381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257972.1:p.Ser369Gly
CA404303504
NM_001271043.2:c.1105A>G