Canonical Allele Identifier: PA2829441789
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg21258Thr
CA310852
NM_003319.4:c.63773G>C