Canonical Allele Identifier: PA2826410251
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr678Ala
CA10581905
NM_001256850.1:c.2032A>G