Canonical Allele Identifier: PA2826416321
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys12739Arg
CA184461
NM_001256850.1:c.38215T>C