Canonical Allele Identifier: PA2830240897
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg23606Ser
CA311019
NM_133437.4:c.70816C>A