Canonical Allele Identifier: PA2829998772
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202267
ClinVar RCV Id: RCV004493679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly1150Ala
CA362324700
NM_022455.5:c.3449G>C