Canonical Allele Identifier: PA645396002
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 391930
ClinVar RCV Id: RCV000421141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257972.1:p.Arg371Gln
CA16608869
NM_001271043.2:c.1112G>A