Canonical Allele Identifier: PA2829983991
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1738Leu
CA10583347
NM_021055.3:c.5213C>T