Canonical Allele Identifier: PA2826414300
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val8460Ile
CA2000027
NM_001256850.1:c.25378G>A