Canonical Allele Identifier: PA2827007060
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207659
ClinVar RCV Id: RCV000189889 RCV000564968 RCV000557687 RCV000768351 RCV001200210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser477Thr
CA031106
NM_001318829.2:c.1430G>C