Canonical Allele Identifier: PA2827012483
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser294Phe
CA030798
NM_001318831.2:c.881C>T