Canonical Allele Identifier: PA2829972114
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238095
ClinVar RCV Id: RCV000231494 RCV000608375 RCV001018094 RCV002500763 RCV004532858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu287Asp
CA056597
NM_021055.3:c.861G>C
CA394314999
NM_021055.3:c.861G>T