Canonical Allele Identifier: PA2829982071
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49956
ClinVar RCV Id: RCV000043223 RCV002298454
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly1536Ser
CA020963
NM_021055.3:c.4606G>A