Canonical Allele Identifier: PA2828412711
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 843014
ClinVar RCV Id: RCV001045541 RCV003307839 RCV003462532 RCV004004778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val886Met
CA276741693
NM_001370404.1:c.2656G>A