Canonical Allele Identifier: PA2827015446
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052237
ClinVar RCV Id: RCV001360380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asp1234Ala
CA394302259
NM_001318831.2:c.3701A>C