Canonical Allele Identifier: PA139732
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47000
ClinVar RCV Id: RCV000040270 RCV000643829 RCV000726230 RCV001132131 RCV001133060 RCV001132132 RCV001132133 RCV001132134 RCV002408534 RCV004534899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly13822Arg
CA139729
NM_001256850.1:c.41464G>A
CA349626930
NM_001256850.1:c.41464G>C