Canonical Allele Identifier: PA2829983686
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu1707Phe
CA022293
NM_021055.3:c.5119C>T