Canonical Allele Identifier: PA658815809
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val25567Phe
CA1989872
NM_001267550.2:c.76699G>T