Canonical Allele Identifier: PA2829983801
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448738
ClinVar RCV Id: RCV000516657 RCV000529988 RCV001023876 RCV001572599 RCV004003590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ser1721Asn
CA276759923
NM_021055.3:c.5162G>A