Canonical Allele Identifier: PA2826412683
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser5134Gly
CA2002044
NM_001256850.1:c.15400A>G