Canonical Allele Identifier: PA1139751748
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 941828
ClinVar RCV Id: RCV003232233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Leu2228Pro
CA362324915
NM_022455.5:c.6683T>C
CA1139659264
NM_022455.5:c.6683_6684delinsCT