Canonical Allele Identifier: PA2825436048
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Met649Thr
CA016283
NM_001077183.3:c.1946T>C