Canonical Allele Identifier: PA2825954848
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Ser208Arg
CA038264
NM_001162426.2:c.622A>C
CA375372403
NM_001162426.2:c.624T>G
CA375372405
NM_001162426.2:c.624T>A