Canonical Allele Identifier: PA2573170592
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469824
ClinVar RCV Id: RCV001973112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1738Cys
CA394314391
NM_000548.5:c.5213C>G