Canonical Allele Identifier: PA309622
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg10698Gln
CA309620
NM_001267550.2:c.32093G>A