Canonical Allele Identifier: PA2825572500
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser211Phe
CA10583283
NM_001114382.3:c.632C>T