Canonical Allele Identifier: PA111149
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159395
ClinVar RCV Id: RCV000286929 RCV000793328 RCV003231294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg2005Gln
CA295024
NM_022455.5:c.6014G>A