Canonical Allele Identifier: PA2829998711
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165986
ClinVar RCV Id: RCV003232805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asp1103Glu
CA132831308
NM_022455.5:c.3309C>G
CA362323584
NM_022455.5:c.3309C>A