Canonical Allele Identifier: PA2829983526
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1694Ala
CA394314331
NM_021055.3:c.5080C>G