Canonical Allele Identifier: PA915959885
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642802
ClinVar RCV Id: RCV000796334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1477Ser
CA276753515
NM_000548.5:c.4431G>C
CA394302236
NM_000548.5:c.4431G>T