ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827011701
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
468193
ClinVar RCV Id:
RCV000541726
RCV002377105
RCV003999344
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305760.1:p.Val119Met
CA394315689
NM_001318831.2:c.355G>A