Canonical Allele Identifier: PA2829715947
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 596675
ClinVar RCV Id: RCV000732584
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_015627.1:p.Phe3Leu
CA355988690
NM_007331.2:c.7T>C
CA355988715
NM_007331.2:c.9T>A
CA355988719
NM_007331.2:c.9T>G