Canonical Allele Identifier: PA2826410698
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala1385Thr
CA181990
NM_001256850.1:c.4153G>A