ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828413353
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
406072
ClinVar RCV Id:
RCV000456897
RCV001020136
RCV001618706
RCV004533165
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001357333.1:p.Arg1083Trp
CA046408
NM_001370404.1:c.3247C>T