Canonical Allele Identifier: PA2829715953
Gene: NSD2 HGNC NCBI
ClinVar RCV:
RCV004493712
ClinVar Variation:
3202300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_015627.1:p.Lys17Asn
CA2811807
NM_007331.2:c.51G>C
CA355989151
NM_007331.2:c.51G>T