Canonical Allele Identifier: PA915987388
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 237715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Asp951Val
CA035584
NM_001162427.2:c.2852A>T