Canonical Allele Identifier: PA2829970269
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207654
ClinVar RCV Id: RCV000189880 RCV000475609 RCV001009700 RCV003996860
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Lys34Thr
CA027975
NM_021055.3:c.101A>C