Canonical Allele Identifier: PA645437907
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436064
ClinVar RCV Id: RCV003231627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ile1976Thr
CA362315804
NM_022455.5:c.5927T>C