ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA269802
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
130686
ClinVar RCV Id:
RCV000118795
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001254479.2:p.Arg32869Pro
CA269799
NM_001267550.2:c.98606G>C