Canonical Allele Identifier: PA2829980706
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405984
ClinVar RCV Id: RCV000469951 RCV001543108 RCV001696845 RCV002318520
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asp1363Asn
CA050657
NM_021055.3:c.4087G>A