Canonical Allele Identifier: PA2573170409
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519233
ClinVar RCV Id: RCV002024455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Tyr1549His
CA394304973
NM_000548.5:c.4645T>C