Canonical Allele Identifier: PA2826158237
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2923716
ClinVar RCV Id: RCV003783274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Ser450Arg
CA373425773
NM_001190384.3:c.1350C>G
CA373425775
NM_001190384.3:c.1350C>A
CA373425785
NM_001190384.3:c.1348A>C