Canonical Allele Identifier: PA2828189802
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_001352831.1:p.Leu60Pro
CA130005
NM_001365902.3:c.179T>C