Canonical Allele Identifier: PA178419
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg31853Cys
CA178417
NM_001267550.2:c.95557C>T