Canonical Allele Identifier: PA310263
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp21265Asn
CA310261
NM_001267550.2:c.63793G>A