Canonical Allele Identifier: PA658664801
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp5774Asn
CA2001859
NM_001267550.2:c.17320G>A