Canonical Allele Identifier: PA2828059492
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Met230Val
CA319232
NM_001362177.1:c.688A>G