Canonical Allele Identifier: PA2830214620
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg7257Cys
CA1994784
NM_133432.3:c.21769C>T