Canonical Allele Identifier: PA2828090604
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro316Gln
CA056703
NM_001363528.2:c.947C>A