Canonical Allele Identifier: PA138705
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46596
ClinVar RCV Id: RCV000039866 RCV000539374 RCV001719762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg4683Cys
CA138702
NM_001256850.1:c.14047C>T