Canonical Allele Identifier: PA2828419778
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074520
ClinVar RCV Id: RCV004014054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Trp1165Cys
CA394291543
NM_001370405.1:c.3495G>C
CA394291545
NM_001370405.1:c.3495G>T