Canonical Allele Identifier: PA174453
Gene: USF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161613
ClinVar RCV Id: RCV000149149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003358.1:p.Arg166Gln
CA174452
NM_003367.4:c.497G>A