Canonical Allele Identifier: PA2826421407
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp22076Tyr
CA1990672
NM_001256850.1:c.66226G>T