Canonical Allele Identifier: PA2827005377
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Met1612Val
CA021857
NM_001318827.2:c.4834A>G