Canonical Allele Identifier: PA2828756886
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 2146077
ClinVar RCV Id: RCV003074378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365333.1:p.Gly415Ser
CA305564152
NM_001378404.1:c.1243G>A