Canonical Allele Identifier: PA2826496320
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His14522Arg
CA1995834
NM_001267550.2:c.43565A>G