Canonical Allele Identifier: PA658814705
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 500219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly18952Val
CA1993173
NM_001267550.2:c.56855G>T