Canonical Allele Identifier: PA2828060234
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Val527Ala
CA030214
NM_001362177.1:c.1580T>C