Canonical Allele Identifier: PA2826425619
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg29431His
CA1987337
NM_001256850.1:c.88292G>A