Canonical Allele Identifier: PA294994
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159381
ClinVar RCV Id: RCV003231281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Trp1954Cys
CA294992
NM_022455.5:c.5862G>C
CA362313786
NM_022455.5:c.5862G>T