Canonical Allele Identifier: PA2826417038
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val14153Ile
CA184456
NM_001256850.1:c.42457G>A