Canonical Allele Identifier: PA2828195989
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 391930
ClinVar RCV Id: RCV000421141
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352913.1:p.Arg362Gln
CA16608869
NM_001365984.2:c.1085G>A