Canonical Allele Identifier: PA2826418449
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu16795Lys
CA178718
NM_001256850.1:c.50383G>A