Canonical Allele Identifier: PA645413504
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Gly1031Arg
CA035781
NM_000368.5:c.3091G>A
CA375367495
NM_000368.5:c.3091G>C