Canonical Allele Identifier: PA181572
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34637Gln
CA181570
NM_001267550.2:c.103910G>A