Canonical Allele Identifier: PA658667309
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg27216His
CA1989175
NM_001267550.2:c.81647G>A