Canonical Allele Identifier: PA2826422384
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly23908Ser
CA1989878
NM_001256850.1:c.71722G>A