Canonical Allele Identifier: PA2826411560
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile2969Val
CA2004477
NM_001256850.1:c.8905A>G