Canonical Allele Identifier: PA139428
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46882
ClinVar RCV Id: RCV000040152 RCV000154080 RCV000241592 RCV000770062 RCV001085855 RCV001133885 RCV001133887 RCV001133886 RCV001133888 RCV001133889 RCV004541146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg10701Gln
CA139426
NM_001256850.1:c.32102G>A