Canonical Allele Identifier: PA916056603
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230395
ClinVar RCV Id: RCV000213113 RCV000537615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ser6Asn
CA033570
NM_021055.3:c.17G>A