Canonical Allele Identifier: PA2826415138
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu10357Pro
CA1998764
NM_001256850.1:c.31070T>C