Canonical Allele Identifier: PA658817308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val35031Met
CA1985308
NM_001267550.2:c.105091G>A