Canonical Allele Identifier: PA645410392
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg19748Gln
CA1992696
NM_001267550.2:c.59243G>A