Canonical Allele Identifier: PA2827008167
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 836706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg850Gly
CA394279410
NM_001318829.2:c.2548A>G