Canonical Allele Identifier: PA891846201
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 574692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro311Ala
CA375368729
NM_000368.5:c.931C>G