Canonical Allele Identifier: PA658814128
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg15218Trp
CA1995385
NM_001267550.2:c.45652C>T