Canonical Allele Identifier: PA2825577572
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1714Ala
CA394314331
NM_001114382.3:c.5140C>G