Canonical Allele Identifier: PA302624
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg22038Lys
CA302622
NM_001256850.1:c.66113G>A