Canonical Allele Identifier: PA2826489440
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 496991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala1914Thr
CA2005144
NM_001267550.2:c.5740G>A