Canonical Allele Identifier: PA2827013050
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50189
ClinVar RCV Id: RCV000043458 RCV000122211 RCV000202889 RCV000574169 RCV001703940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Met449Thr
CA016283
NM_001318831.2:c.1346T>C