Canonical Allele Identifier: PA645437901
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 431827
ClinVar RCV Id: RCV000498391
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Glu1970Asp
CA362315704
NM_022455.5:c.5910G>C
CA362315706
NM_022455.5:c.5910G>T