Canonical Allele Identifier: PA645433103
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val1073Met
CA044793
NM_000548.5:c.3217G>A