Canonical Allele Identifier: PA2826419201
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly18160Asp
CA1992669
NM_001256850.1:c.54479G>A