Canonical Allele Identifier: PA2573282680
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513551
ClinVar RCV Id: RCV003232515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly2013Arg
CA362316220
NM_022455.5:c.6037G>A
CA362316224
NM_022455.5:c.6037G>C