Canonical Allele Identifier: PA2741981594
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2573818
ClinVar RCV Id: RCV003318154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asn1333Asp
CA362340005
NM_022455.5:c.3997A>G