Canonical Allele Identifier: PA658815054
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu20871Val
CA1992201
NM_001267550.2:c.62611C>G