Canonical Allele Identifier: PA658816860
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 498721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32058Trp
CA1986809
NM_001267550.2:c.96172C>T