Canonical Allele Identifier: PA310717
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg26723Gln
CA310716
NM_001256850.1:c.80168G>A