Canonical Allele Identifier: PA2826489517
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg2501Gln
CA2004801
NM_001267550.2:c.7502G>A