Canonical Allele Identifier: PA2826419854
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys19398Thr
CA10587487
NM_001256850.1:c.58193A>C