Canonical Allele Identifier: PA2829983746
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318336
ClinVar RCV Id: RCV000373763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu1713Gly
CA10643155
NM_021055.3:c.5138A>G