Canonical Allele Identifier: PA2829442702
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 228169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val22652Ile
CA1986999
NM_003319.4:c.67954G>A