Canonical Allele Identifier: PA302604
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192143
ClinVar RCV Id: RCV000172619 RCV000213505 RCV000244689 RCV001080503 RCV001132342 RCV001129598 RCV001129600 RCV001129597 RCV001129599 RCV001171247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser29361Ile
CA302602
NM_001256850.1:c.88082G>T