Canonical Allele Identifier: PA309681
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg11150Gln
CA309680
NM_001256850.1:c.33449G>A