Canonical Allele Identifier: PA178428
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165717
ClinVar RCV Id: RCV000152182 RCV000477611 RCV000726542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg28987His
CA178427
NM_133378.4:c.86960G>A