Canonical Allele Identifier: PA310673
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg27528Trp
CA310671
NM_001267550.2:c.82582C>T