Canonical Allele Identifier: PA183826
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179154
ClinVar RCV Id: RCV000155940 RCV000172202 RCV000322052 RCV000264757 RCV000270671 RCV000361658 RCV000362406 RCV000768866 RCV002362825
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val28937Ile
CA183824
NM_001256850.1:c.86809G>A