Canonical Allele Identifier: PA2830190823
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala1081Val
CA2005593
NM_133378.4:c.3242C>T