Canonical Allele Identifier: PA2828059526
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Pro245Leu
CA027020
NM_001362177.1:c.734C>T