Canonical Allele Identifier: PA2827007689
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile674Phe
CA10583306
NM_001318829.2:c.2020A>T