Canonical Allele Identifier: PA645411169
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly26516Ser
CA1989460
NM_001267550.2:c.79546G>A