Canonical Allele Identifier: PA2829846138
Gene: NFU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 488564
ClinVar RCV Id: RCV000578338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056515.2:p.Arg158Trp
CA347123810
NM_015700.4:c.472C>T