ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829982769
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000055369
RCV001342211
RCV002336203
ClinVar Variation:
65153
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066399.2:p.Val1630Phe
CA021508
NM_021055.3:c.4888G>T