Canonical Allele Identifier: PA130006
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 36966
ClinVar RCV Id: RCV000030646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002492.2:p.Leu60Pro
CA130005
NM_002501.4:c.179T>C