Canonical Allele Identifier: PA294965
Gene: NSD1 HGNC NCBI
ClinVar RCV:
RCV003231270
ClinVar Variation:
159370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg1811Gln
CA294963
NM_022455.5:c.5432G>A