Canonical Allele Identifier: PA262445
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu362Pro
CA013704
NM_000548.5:c.1085T>C