Canonical Allele Identifier: PA2830201323
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala27283Asp
CA1987895
NM_133378.4:c.81848C>A