Canonical Allele Identifier: PA183827
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179154
ClinVar RCV Id: RCV000155940 RCV000172202 RCV000322052 RCV000264757 RCV000270671 RCV000361658 RCV000362406 RCV000768866 RCV002362825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val30578Ile
CA183824
NM_001267550.2:c.91732G>A