Canonical Allele Identifier: PA2826413549
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val6924Ile
CA2000959
NM_001256850.1:c.20770G>A