Canonical Allele Identifier: PA2825958067
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Pro1087His
CA036822
NM_001162427.2:c.3260C>A