Canonical Allele Identifier: PA658809345
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 524699
ClinVar RCV Id: RCV003231551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys2183Gly
CA362323882
NM_022455.5:c.6547T>G