Canonical Allele Identifier: PA2828410299
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184186
ClinVar RCV Id: RCV000163373 RCV000190050 RCV000765260 RCV001086110 RCV003995252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asn187Ser
CA022534
NM_001370404.1:c.560A>G