Canonical Allele Identifier: PA2826410087
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala405Thr
CA179430
NM_001256850.1:c.1213G>A