Canonical Allele Identifier: PA1139751726
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 975312
ClinVar RCV Id: RCV003232268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Glu2217Asp
CA362324636
NM_022455.5:c.6651G>C
CA362324638
NM_022455.5:c.6651G>T