Canonical Allele Identifier: PA2499252746
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Ser87Arg
CA038264
NM_001362177.1:c.259A>C
CA375372403
NM_001362177.1:c.261T>G
CA375372405
NM_001362177.1:c.261T>A