Canonical Allele Identifier: PA658817431
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 534963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu35796Ala
CA349401143
NM_001267550.2:c.107387A>C