ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825575770
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000043035
RCV000190021
RCV000190880
RCV002453340
RCV002490595
RCV004537174
ClinVar Variation:
49770
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001107854.1:p.Arg1200Trp
CA019313
NM_001114382.3:c.3598C>T