Canonical Allele Identifier: PA645412759
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34761Gln
CA1985448
NM_001267550.2:c.104282G>A