Canonical Allele Identifier: PA2826419173
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly18109Ser
CA231599
NM_001256850.1:c.54325G>A