Canonical Allele Identifier: PA2825577470
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Met1692Val
CA021857
NM_001114382.3:c.5074A>G