Canonical Allele Identifier: PA2828411980
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535866
ClinVar RCV Id: RCV000644078 RCV001014102 RCV000765268 RCV004003988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala675Ser
CA276737715
NM_001370404.1:c.2023G>T