Canonical Allele Identifier: PA2573095261
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1319639
ClinVar RCV Id: RCV003237632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ala2256Gly
CA362325714
NM_022455.5:c.6767C>G