Canonical Allele Identifier: PA2828195883
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 546383
ClinVar RCV Id: RCV000658249
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352913.1:p.Asp108Ala
CA404314300
NM_001365984.2:c.323A>C