Canonical Allele Identifier: PA645433220
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405981
ClinVar RCV Id: RCV000461553 RCV001019998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala1110Gly
CA16614990
NM_000548.5:c.3329C>G