Canonical Allele Identifier: PA2828061156
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Gly910Arg
CA035781
NM_001362177.1:c.2728G>A
CA375367495
NM_001362177.1:c.2728G>C