Canonical Allele Identifier: PA2826416148
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg12378His
CA183622
NM_001256850.1:c.37133G>A