Canonical Allele Identifier: PA2830274997
Gene: NUP98 HGNC NCBI

Linked Data

ClinVar Variation Id: 375277
ClinVar RCV Id: RCV000416348
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_624358.2:p.Asn1662Ser
CA16044029
NM_139132.4:c.4985A>G