Canonical Allele Identifier: PA2828093549
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718047
ClinVar RCV Id: RCV002304844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser1174Arg
CA394291960
NM_001363528.2:c.3520A>C
CA394291979
NM_001363528.2:c.3522C>A
CA394291987
NM_001363528.2:c.3522C>G