ClinGen Allele Registry
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Canonical Allele Identifier:
PA223687
Gene: NSD1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000723729
RCV002336237
RCV003231139
RCV003935069
ClinVar Variation:
96061
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_071900.2:p.Lys1631Arg
CA223685
NM_022455.5:c.4892A>G