Canonical Allele Identifier: PA2825954992
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Ala122Val
CA037947
NM_001162427.2:c.365C>T