Canonical Allele Identifier: PA2829431868
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn4294His
CA142026
NM_003319.4:c.12880A>C