Canonical Allele Identifier: PA645438011
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235572
ClinVar RCV Id: RCV000224225 RCV003231409
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly2585Arg
CA3578176
NM_022455.5:c.7753G>A
CA362334421
NM_022455.5:c.7753G>C