Canonical Allele Identifier: PA2825958113
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Asn1106Asp
CA319266
NM_001162427.2:c.3316A>G