Canonical Allele Identifier: PA2828756858
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 2500469
ClinVar RCV Id: RCV003225381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365333.1:p.Ser353Gly
CA404303504
NM_001378404.1:c.1057A>G