Canonical Allele Identifier: PA2826412381
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala4529Thr
CA2002382
NM_001256850.1:c.13585G>A