Canonical Allele Identifier: PA2826420479
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala20503Thr
CA1991530
NM_001256850.1:c.61507G>A