Canonical Allele Identifier: PA2741981725
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2636297
ClinVar RCV Id: RCV003393138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Thr2234Ser
CA362325068
NM_022455.5:c.6700A>T
CA362325079
NM_022455.5:c.6701C>G