Canonical Allele Identifier: PA139438
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46888
ClinVar RCV Id: RCV000040158 RCV000172680 RCV000770057 RCV001130091 RCV001130090 RCV001130092 RCV001135119 RCV001135120 RCV001082271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg10822Thr
CA139436
NM_001256850.1:c.32465G>C