Canonical Allele Identifier: PA2827000379
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_001305756.1:p.Asn150Ser
CA022534
NM_001318827.2:c.449A>G