Canonical Allele Identifier: PA208677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg5743Trp
CA208675
NM_001267550.2:c.17227C>T