ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA179027
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
166235
ClinVar RCV Id:
RCV000152418
RCV000643407
RCV002326875
RCV001358499
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_597676.3:p.Cys4059Gly
CA179026
NM_133432.3:c.12175T>G