Canonical Allele Identifier: PA2827009794
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1400703
ClinVar RCV Id: RCV001911450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1421Arg
CA394304672
NM_001318829.2:c.4262A>G