Canonical Allele Identifier: PA2830199148
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263494
ClinVar RCV Id: RCV000243281 RCV000603891 RCV000643619 RCV000769944 RCV001132751 RCV001132752 RCV001132753 RCV001132754 RCV001132755 RCV001532417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gln22113Arg
CA1990272
NM_133378.4:c.66338A>G