Canonical Allele Identifier: PA645434076
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1401Ala
CA050641
NM_000548.5:c.4201C>G