Canonical Allele Identifier: PA2829445529
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg25978Cys
CA141711
NM_003319.4:c.77932C>T