Canonical Allele Identifier: PA891851279
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 567561
ClinVar RCV Id: RCV003231579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys2124Gly
CA362320626
NM_022455.5:c.6370T>G