Canonical Allele Identifier: PA2827011523
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 843014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val837Met
CA276741693
NM_001318829.2:c.2509G>A