Canonical Allele Identifier: PA645437998
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 352891
ClinVar RCV Id: RCV000762247 RCV003231452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser2342Leu
CA3578073
NM_022455.5:c.7025C>T