Canonical Allele Identifier: PA658659696
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Gly680Arg
CA030742
NM_000368.5:c.2038G>A
CA375361224
NM_000368.5:c.2038G>C