Canonical Allele Identifier: PA2826412885
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly5549Cys
CA2001786
NM_001256850.1:c.16645G>T