Canonical Allele Identifier: PA645437822
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436063
ClinVar RCV Id: RCV003231510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro1690Arg
CA362303073
NM_022455.5:c.5069C>G