Canonical Allele Identifier: PA658813104
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 74283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser7531Asn
CA2000803
NM_001267550.2:c.22592G>A