Canonical Allele Identifier: PA2825182197
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gly671Ser
CA394274467
NM_000548.5:c.2011G>A