Canonical Allele Identifier: PA2826423580
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg26004His
CA1988998
NM_001256850.1:c.78011G>A