Canonical Allele Identifier: PA2829436906
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg13255Cys
CA1991397
NM_003319.4:c.39763C>T