Canonical Allele Identifier: PA2826411118
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp2140Glu
CA2005052
NM_001256850.1:c.6420T>A
CA349439525
NM_001256850.1:c.6420T>G