ClinGen Allele Registry
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Canonical Allele Identifier:
PA149220
Gene: NSD1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000082144
RCV001573769
RCV002311714
RCV003231152
ClinVar Variation:
96079
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_071900.2:p.Ala2546Thr
CA149218
NM_022455.5:c.7636G>A