Canonical Allele Identifier: PA2828092791
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207675
ClinVar RCV Id: RCV000189913 RCV001017697 RCV000807950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg947Gly
CA043555
NM_001363528.2:c.2839A>G