Canonical Allele Identifier: PA645409312
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp8706Asn
CA2000074
NM_001267550.2:c.26116G>A