Canonical Allele Identifier: PA2828092969
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 936312
ClinVar RCV Id: RCV001205088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1006Gln
CA394285219
NM_001363528.2:c.3016G>C