Canonical Allele Identifier: PA138765
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46615
ClinVar RCV Id: RCV000039885 RCV000172406 RCV001130571 RCV001130572 RCV001130573 RCV001130570 RCV001135657 RCV001080301 RCV003149638 RCV004541134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys4194Arg
CA138763
NM_133378.4:c.12581A>G