Canonical Allele Identifier: PA645411188
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg26628Gln
CA1989421
NM_001267550.2:c.79883G>A