Canonical Allele Identifier: PA2826421440
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg22126Gln
CA1990652
NM_001256850.1:c.66377G>A