ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825572820
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000732320
RCV001086904
RCV002255384
RCV004000681
ClinVar Variation:
405962
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001107854.1:p.Arg308Trp
CA056666
NM_001114382.3:c.922C>T