Canonical Allele Identifier: PA111202
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4140
ClinVar RCV Id: RCV003231082
ClinVar Variation Id: 2571813
ClinVar RCV Id: RCV003313522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys2183Ser
CA281542
NM_022455.5:c.6548G>C
CA362323877
NM_022455.5:c.6547T>A