Canonical Allele Identifier: PA2825401077
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662722
ClinVar RCV Id: RCV003441387
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035889.1:p.Leu10Phe
CA355988898
NM_001042424.3:c.28C>T