Canonical Allele Identifier: PA295003
Gene: NSD1 HGNC NCBI
ClinVar RCV:
RCV003231286
ClinVar Variation:
159387
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly1973Val
CA295001
NM_022455.5:c.5918G>T