Canonical Allele Identifier: PA645435264
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Lys1658Arg
CA16615040
NM_000548.5:c.4973A>G