Canonical Allele Identifier: PA2828091857
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala673Val
CA035710
NM_001363528.2:c.2018C>T