Canonical Allele Identifier: PA223657
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96046
ClinVar RCV Id: RCV000082111 RCV003258665 RCV003231127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Met800Thr
CA223655
NM_022455.5:c.2399T>C