Canonical Allele Identifier: PA2829978379
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405964
ClinVar RCV Id: RCV000469143 RCV000574231
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1035Trp
CA044888
NM_021055.3:c.3103C>T
CA645573330
NM_021055.3:c.3102_3103delinsTT