Canonical Allele Identifier: PA2825956658
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 48861
ClinVar Variation Id: 1492044
ClinVar RCV Id: RCV001989095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Asp607Glu
CA005685
NM_001162427.2:c.1821C>G
CA375362316
NM_001162427.2:c.1821C>A