Canonical Allele Identifier: PA645409999
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229446
ClinVar RCV Id: RCV000218703 RCV001135634 RCV001134133 RCV001135635 RCV001135633 RCV001135636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16376Cys
CA1994670
NM_001267550.2:c.49126C>T