Canonical Allele Identifier: PA2827016604
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 514715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gln1535Arg
CA055149
NM_001318831.2:c.4604A>G