Canonical Allele Identifier: PA645409473
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg10464Trp
CA1998969
NM_001267550.2:c.31390C>T