Canonical Allele Identifier: PA2827009339
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1286Ala
CA050641
NM_001318829.2:c.3856C>G