Canonical Allele Identifier: PA1139750770
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 930466
ClinVar RCV Id: RCV003232224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Lys237Glu
CA362295310
NM_022455.5:c.709A>G