Canonical Allele Identifier: PA2828415527
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro1693Ala
CA394314331
NM_001370404.1:c.5077C>G