Canonical Allele Identifier: PA2826417398
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val14796Asp
CA1994638
NM_001256850.1:c.44387T>A