Canonical Allele Identifier: PA2829442999
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 498721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg22993Trp
CA1986809
NM_003319.4:c.68977C>T