Canonical Allele Identifier: PA916002948
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_001257972.1:p.Leu68Pro
CA130005
NM_001271043.2:c.203T>C