Canonical Allele Identifier: PA2826409921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu143Lys
CA2006320
NM_001256850.1:c.427G>A