Canonical Allele Identifier: PA658665707
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16186Cys
CA1994792
NM_001267550.2:c.48556C>T