Canonical Allele Identifier: PA915953495
Gene: NFU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 488564
ClinVar RCV Id: RCV000578338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002756.1:p.Arg41Trp
CA347123810
NM_001002756.2:c.121C>T