Canonical Allele Identifier: PA284258
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Lys3154Arg
CA284252
NM_133379.5:c.9461A>G