Canonical Allele Identifier: PA645413111
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Met209Val
CA038277
NM_000368.5:c.625A>G