Canonical Allele Identifier: PA139439
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_001254479.2:p.Arg11139Thr
CA139436
NM_001267550.2:c.33416G>C