Canonical Allele Identifier: PA2828419491
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406072
ClinVar RCV Id: RCV000456897 RCV001020136 RCV001618706 RCV004533165
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1084Trp
CA046408
NM_001370405.1:c.3250C>T