Canonical Allele Identifier: PA234439
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 167393
ClinVar RCV Id: RCV000153610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro1119Ala
CA234437
NM_022455.5:c.3355C>G