Canonical Allele Identifier: PA2825401095
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2535770
ClinVar RCV Id: RCV003261209
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035889.1:p.Ala70Asp
CA2811836
NM_001042424.3:c.209C>A