Canonical Allele Identifier: PA2827013165
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala475Thr
CA10583300
NM_001318831.2:c.1423G>A