Canonical Allele Identifier: PA2827018934
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 390104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1125Ala
CA046994
NM_001318832.2:c.3373C>G