Canonical Allele Identifier: PA658659914
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro1138His
CA036822
NM_000368.5:c.3413C>A