Canonical Allele Identifier: PA658665338
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 451457
ClinVar RCV Id: RCV000521971 RCV003231516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly2155Arg
CA362321156
NM_022455.5:c.6463G>A
CA362321158
NM_022455.5:c.6463G>C