Canonical Allele Identifier: PA223644
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96037
ClinVar RCV Id: RCV000082102 RCV002390241 RCV003231120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asn556Asp
CA223642
NM_022455.5:c.1666A>G