Canonical Allele Identifier: PA658816379
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 519091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28439Trp
CA1988664
NM_001267550.2:c.85315C>T