Canonical Allele Identifier: PA2829975130
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala673Val
CA035710
NM_021055.3:c.2018C>T