Canonical Allele Identifier: PA2826418952
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg17717Cys
CA208075
NM_001256850.1:c.53149C>T