Canonical Allele Identifier: PA2826414289
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly8444Ser
CA2000037
NM_001256850.1:c.25330G>A