Canonical Allele Identifier: PA141011
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47441
ClinVar RCV Id: RCV000040710 RCV000176789 RCV000531860 RCV000852801 RCV002354203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gln25740Pro
CA141009
NM_133378.4:c.77219A>C