Canonical Allele Identifier: PA2830234521
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg13447Cys
CA1991397
NM_133437.4:c.40339C>T