Canonical Allele Identifier: PA645411062
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly25549Ser
CA1989878
NM_001267550.2:c.76645G>A