ClinGen Allele Registry
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Canonical Allele Identifier:
PA916056642
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000471856
RCV001797088
RCV002436401
RCV004000706
RCV004533162
ClinVar Variation:
406038
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066399.2:p.Pro94Leu
CA042049
NM_021055.3:c.281C>T