Canonical Allele Identifier: PA2829982299
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497447
ClinVar RCV Id: RCV003213902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Met1572Val
CA394308148
NM_021055.3:c.4714A>G