Canonical Allele Identifier: PA2826415788
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu11650Lys
CA1996692
NM_001256850.1:c.34948G>A