Canonical Allele Identifier: PA2829973448
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu498Lys
CA014970
NM_021055.3:c.1492G>A