Canonical Allele Identifier: PA2829998642
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3234878
ClinVar RCV Id: RCV004547226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro1060Ala
CA362322527
NM_022455.5:c.3178C>G