Canonical Allele Identifier: PA141516
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg33145Gln
CA141513
NM_001267550.2:c.99434G>A