Canonical Allele Identifier: PA2829715948
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348417
ClinVar RCV Id: RCV001309481 RCV004021960
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_015627.1:p.Ser4Asn
CA2811799
NM_007331.2:c.11G>A