Canonical Allele Identifier: PA2826417136
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile14339Val
CA1994939
NM_001256850.1:c.43015A>G