Canonical Allele Identifier: PA2826410525
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala1081Val
CA2005593
NM_001256850.1:c.3242C>T