Canonical Allele Identifier: PA2828060257
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_001349106.1:p.Asp537Glu
CA005685
NM_001362177.1:c.1611C>G
CA375362316
NM_001362177.1:c.1611C>A