Canonical Allele Identifier: PA2827020458
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Met1559Arg
CA394308151
NM_001318832.2:c.4676T>G