Canonical Allele Identifier: PA916023972
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65074
ClinVar RCV Id: RCV000055281 RCV001853092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala900Pro
CA017834
NM_001318832.2:c.2698G>C