Canonical Allele Identifier: PA2829984163
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1747Met
CA022424
NM_021055.3:c.5239G>A