Canonical Allele Identifier: PA302451
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu22408Pro
CA302449
NM_001256850.1:c.67223T>C