Canonical Allele Identifier: PA2826489619
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 509244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn3430His
CA2004146
NM_001267550.2:c.10288A>C