Canonical Allele Identifier: PA2825576662
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1474Ser
CA020513
NM_001114382.3:c.4420C>T