Canonical Allele Identifier: PA2825438471
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1383Ala
CA050903
NM_001077183.3:c.4147C>G