Canonical Allele Identifier: PA2830239407
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg21450Thr
CA310852
NM_133437.4:c.64349G>C