Canonical Allele Identifier: PA2827001467
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64992
ClinVar RCV Id: RCV000055196 RCV000547543 RCV003298099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.His485Tyr
CA015081
NM_001318827.2:c.1453C>T