Canonical Allele Identifier: PA658668638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34859Trp
CA60956099
NM_001267550.2:c.104575C>T