Canonical Allele Identifier: PA658809155
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 524694
ClinVar RCV Id: RCV003231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asn272Lys
CA3576960
NM_022455.5:c.816C>A
CA362295887
NM_022455.5:c.816C>G