Canonical Allele Identifier: PA2827007363
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 385710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala574Val
CA16608037
NM_001318829.2:c.1721C>T