Canonical Allele Identifier: PA645410417
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg19950Gln
CA1992597
NM_001267550.2:c.59849G>A