ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA100058
Gene: TTR
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000014371
RCV000030571
RCV000030572
RCV000517494
RCV002415415
RCV002415438
RCV003480030
ClinVar Variation:
13429
36889
36890
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000362.1:p.Ser70Arg
CA256808
NM_000371.3:c.210T>G
CA260564
NM_000371.3:c.208A>C
CA260565
NM_000371.3:c.210T>A