Canonical Allele Identifier: PA2828421298
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 424444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Val1603Met
CA16620103
NM_001370405.1:c.4807G>A