Canonical Allele Identifier: PA2826531697
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 452926
ClinVar RCV Id: RCV000519161 RCV001263215 RCV003766975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257973.1:p.Met40Lys
CA404313335
NM_001271044.3:c.119T>A