Canonical Allele Identifier: PA141438
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32473His
CA141434
NM_001267550.2:c.97418G>A