Canonical Allele Identifier: PA2829715953
Gene: NSD2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

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