Canonical Allele Identifier: PA645437718
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3068762
ClinVar RCV Id: RCV003994822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Lys1133Glu
CA10624121
NM_022455.5:c.3397A>G