Canonical Allele Identifier: PA2828095397
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1683Gln
CA394314713
NM_001363528.2:c.5048G>A