Canonical Allele Identifier: PA2828195653
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 2500469
ClinVar RCV Id: RCV003225381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352911.1:p.Ser320Gly
CA404303504
NM_001365982.2:c.958A>G