Canonical Allele Identifier: PA1139751742
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861947
ClinVar RCV Id: RCV001068574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro2223Ser
CA362324802
NM_022455.5:c.6667C>T