Canonical Allele Identifier: PA311870
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg6058Cys
CA311868
NM_001267550.2:c.18172C>T