Canonical Allele Identifier: PA2825918869
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411270

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Asp871His
CA16612739
NM_001162426.2:c.2611G>C