ClinGen Allele Registry
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Canonical Allele Identifier:
PA223694
Gene: NSD1
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000493737
RCV001818251
RCV003156070
RCV003231143
ClinVar Variation:
96065
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_071900.2:p.Tyr2058Cys
CA223692
NM_022455.5:c.6173A>G