Canonical Allele Identifier: PA2827020936
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1681Ala
CA394314331
NM_001318832.2:c.5041C>G