Canonical Allele Identifier: PA2828168439
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_001352057.1:p.Asn1719Ser
CA16044029
NM_001365128.2:c.5156A>G