Canonical Allele Identifier: PA645480029
Gene: NUP98 HGNC NCBI

Linked Data

ClinVar Variation Id: 375277
ClinVar RCV Id: RCV000416348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057404.2:p.Asn1736Ser
CA16044029
NM_016320.5:c.5207A>G