Canonical Allele Identifier: PA2825956278
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Ala511Gly
CA005191
NM_001162427.2:c.1532C>G