Canonical Allele Identifier: PA658664441
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala3552Pro
CA2004068
NM_001267550.2:c.10654G>C