Canonical Allele Identifier: PA311947
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys7001Arg
CA311945
NM_001267550.2:c.21002A>G