Canonical Allele Identifier: PA294914
Gene: NSD1 HGNC NCBI
ClinVar RCV:
RCV003231247
ClinVar Variation:
159347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys1619Ser
CA294912
NM_022455.5:c.4855T>A
CA362355439
NM_022455.5:c.4856G>C