Canonical Allele Identifier: PA2826428848
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val33562Ala
CA1985231
NM_001256850.1:c.100685T>C