Canonical Allele Identifier: PA2829977175
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro878Ser
CA017740
NM_021055.3:c.2632C>T