Canonical Allele Identifier: PA223650
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96041
ClinVar RCV Id: RCV000082106 RCV003231123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gln610Arg
CA223648
NM_022455.5:c.1829A>G