Canonical Allele Identifier: PA2826429391
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 534963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu34155Ala
CA349401143
NM_001256850.1:c.102464A>C