Canonical Allele Identifier: PA279913
Gene: NUP107 HGNC NCBI

Linked Data

ClinVar Variation Id: 219130
ClinVar RCV Id: RCV000203505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065134.1:p.Asp157Tyr
CA279912
NM_020401.4:c.469G>T