Canonical Allele Identifier: PA2827010538
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486616
ClinVar RCV Id: RCV000561599 RCV000609138 RCV000798867 RCV003736826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1656Ala
CA055040
NM_001318829.2:c.4966C>G