Canonical Allele Identifier: PA2825576636
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486695
ClinVar RCV Id: RCV000565264 RCV001859982
ClinVar Variation Id: 1398873
ClinVar RCV Id: RCV001915287 RCV002331423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1467Asp
CA394302506
NM_001114382.3:c.4401G>C
CA394302508
NM_001114382.3:c.4401G>T