Canonical Allele Identifier: PA645411123
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile26124Asn
CA1989615
NM_001267550.2:c.78371T>A