Canonical Allele Identifier: PA916023188
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile55Met
CA319579
NM_001318832.2:c.165A>G