Canonical Allele Identifier: PA140418
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp22225Asn
CA140414
NM_001267550.2:c.66673G>A