Canonical Allele Identifier: PA645410973
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_001254479.2:p.Gln24681Arg
CA1990272
NM_001267550.2:c.74042A>G