Canonical Allele Identifier: PA2828094872
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Met1549Arg
CA394308151
NM_001363528.2:c.4646T>G