Canonical Allele Identifier: PA2829998562
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2623351
ClinVar RCV Id: RCV003383759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asp1004Glu
CA3577357
NM_022455.5:c.3012C>A
CA362321574
NM_022455.5:c.3012C>G