Canonical Allele Identifier: PA2827005665
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2840486
ClinVar RCV Id: RCV003628370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr1677Ala
CA394315648
NM_001318827.2:c.5029A>G