Canonical Allele Identifier: PA2828090937
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro419Ser
CA014179
NM_001363528.2:c.1255C>T