Canonical Allele Identifier: PA2828417331
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Val461Met
CA319441
NM_001370405.1:c.1381G>A