Canonical Allele Identifier: PA645409802
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 285627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg14679Gln
CA1995765
NM_001267550.2:c.44036G>A