Canonical Allele Identifier: PA2826414618
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser9067Cys
CA1999652
NM_001256850.1:c.27200C>G