Canonical Allele Identifier: PA2827330917
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_001317121.1:p.Asp128Tyr
CA279912
NM_001330192.2:c.382G>T