Canonical Allele Identifier: PA645412290
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp32229Asn
CA1986725
NM_001267550.2:c.96685G>A