Canonical Allele Identifier: PA2829998776
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202268
ClinVar RCV Id: RCV004493680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Val1155Leu
CA362324806
NM_022455.5:c.3463G>C
CA362324807
NM_022455.5:c.3463G>T