Canonical Allele Identifier: PA645409581
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg12131Cys
CA1997504
NM_001267550.2:c.36391C>T