Canonical Allele Identifier: PA1139688979
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 946370
ClinVar RCV Id: RCV001217227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr979Ile
CA044645
NM_001318827.2:c.2936C>T