Canonical Allele Identifier: PA916024045
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu994Pro
CA018468
NM_001318832.2:c.2981T>C