Canonical Allele Identifier: PA2825434121
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Lys34Thr
CA027975
NM_001077183.3:c.101A>C