Canonical Allele Identifier: PA2830224566
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg23539Ser
CA311019
NM_133432.3:c.70615C>A