Canonical Allele Identifier: PA2828415432
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49352
ClinVar RCV Id: RCV000042612 RCV000190040 RCV001797601
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu1673Pro
CA021894
NM_001370404.1:c.5018T>C