Canonical Allele Identifier: PA645411490
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg27877Cys
CA1988894
NM_001267550.2:c.83629C>T