Canonical Allele Identifier: PA295068
Gene: NSD1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asp2126Val
CA295066
NM_022455.5:c.6377A>T