Canonical Allele Identifier: PA2826415168
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val10405Ile
CA1998714
NM_001256850.1:c.31213G>A