Canonical Allele Identifier: PA658666570
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg22320Cys
CA1991397
NM_001267550.2:c.66958C>T