Canonical Allele Identifier: PA2829715952
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202292
ClinVar RCV Id: RCV004493704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_015627.1:p.Ser11Cys
CA2811801
NM_007331.2:c.32C>G