Canonical Allele Identifier: PA2829983361
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406062
ClinVar RCV Id: RCV000658430 RCV001086881 RCV002257695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Met1678Val
CA054307
NM_021055.3:c.5032A>G