Canonical Allele Identifier: PA2825438167
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1291Ala
CA10583332
NM_001077183.3:c.3871C>G