Canonical Allele Identifier: PA645432093
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 385710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala623Val
CA16608037
NM_000548.5:c.1868C>T