Canonical Allele Identifier: PA2829975225
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val679Met
CA035939
NM_021055.3:c.2035G>A