Canonical Allele Identifier: PA295107
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159432
ClinVar RCV Id: RCV003231330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys2202Ser
CA295105
NM_022455.5:c.6604T>A
CA362324281
NM_022455.5:c.6605G>C