Canonical Allele Identifier: PA658815000
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His20557Arg
CA349470323
NM_001267550.2:c.61670A>G