Canonical Allele Identifier: PA107669
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49961
ClinVar RCV Id: RCV000043228 RCV003511996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1743Pro
CA022224
NM_000548.5:c.5228G>C