ClinGen Allele Registry
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Canonical Allele Identifier:
PA294917
Gene: NSD1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
168200
ClinVar RCV:
RCV003231248
ClinVar Variation:
159348
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_071900.2:p.Cys1619Gly
CA294915
NM_022455.5:c.4855T>G