Canonical Allele Identifier: PA295064
Gene: NSD1 HGNC NCBI
ClinVar RCV:
RCV003231312
ClinVar Variation:
159413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asp2119Gly
CA295062
NM_022455.5:c.6356A>G