Canonical Allele Identifier: PA2830230709
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu3974Ala
CA2002711
NM_133437.4:c.11921A>C