Canonical Allele Identifier: PA2826426613
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30907Cys
CA181600
NM_001256850.1:c.92719C>T