Canonical Allele Identifier: PA2826419462
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala18685Thr
CA1992418
NM_001256850.1:c.56053G>A