Canonical Allele Identifier: PA2830200638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg25754Cys
CA310710
NM_133378.4:c.77260C>T