Canonical Allele Identifier: PA2829975185
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2169263
ClinVar RCV Id: RCV003082988
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro677Ser
CA394274535
NM_021055.3:c.2029C>T