Canonical Allele Identifier: PA2499289244
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1036621
ClinVar RCV Id: RCV003232316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro785Thr
CA362315544
NM_022455.5:c.2353C>A
CA1603475958
NM_022455.5:c.2352_2353delinsAA