Canonical Allele Identifier: PA237865
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg19561His
CA237864
NM_133378.4:c.58682G>A