Canonical Allele Identifier: PA2826411536
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val2930Ile
CA238228
NM_001256850.1:c.8788G>A