Canonical Allele Identifier: PA311802
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg139Gln
CA311799
NM_001267550.2:c.416G>A