Canonical Allele Identifier: PA234446
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 167395
ClinVar RCV Id: RCV000153613 RCV003231346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ala2691Thr
CA234444
NM_022455.5:c.8071G>A