Canonical Allele Identifier: PA658815039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20823His
CA1992222
NM_001267550.2:c.62468G>A