Canonical Allele Identifier: PA302488
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg15697Cys
CA302485
NM_001267550.2:c.47089C>T