Canonical Allele Identifier: PA295041
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159401
ClinVar RCV Id: RCV003231300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys2027Ser
CA295039
NM_022455.5:c.6080G>C
CA362316440
NM_022455.5:c.6079T>A