Canonical Allele Identifier: PA2828089787
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val67Ile
CA035477
NM_001363528.2:c.199G>A