Canonical Allele Identifier: PA2830239103
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala20978Asp
CA1987895
NM_133437.4:c.62933C>A