Canonical Allele Identifier: PA310712
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28322Cys
CA310710
NM_001267550.2:c.84964C>T