Canonical Allele Identifier: PA645412065
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg31072His
CA1987337
NM_001267550.2:c.93215G>A