Canonical Allele Identifier: PA2827009082
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1206Val
CA019757
NM_001318829.2:c.3617A>T