Canonical Allele Identifier: PA295035
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159399
ClinVar RCV Id: RCV001561957 RCV003231298
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asn2020Ser
CA295033
NM_022455.5:c.6059A>G