Canonical Allele Identifier: PA658665975
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn18663Ser
CA1993349
NM_001267550.2:c.55988A>G