Canonical Allele Identifier: PA2825183620
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ile885Met
CA394279216
NM_000548.5:c.2655C>G