Canonical Allele Identifier: PA2580454608
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722453
ClinVar RCV Id: RCV002302567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly2209Arg
CA362324437
NM_022455.5:c.6625G>A
CA362324438
NM_022455.5:c.6625G>C