Canonical Allele Identifier: PA2827002086
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu644Gln
CA10583301
NM_001318827.2:c.1931T>A