Canonical Allele Identifier: PA2826426153
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30212Cys
CA178417
NM_001256850.1:c.90634C>T