Canonical Allele Identifier: PA2828059507
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1420507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Pro237Leu
CA375367667
NM_001362177.1:c.710C>T