Canonical Allele Identifier: PA2828418037
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405983
ClinVar RCV Id: RCV000463315 RCV001013872 RCV004000685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Lys657Gln
CA035326
NM_001370405.1:c.1969A>C