Canonical Allele Identifier: PA295028
Gene: NSD1 HGNC NCBI
ClinVar RCV:
RCV003231295
ClinVar Variation:
159396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Tyr2015His
CA295026
NM_022455.5:c.6043T>C