Canonical Allele Identifier: PA2830213841
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1778491
ClinVar RCV Id: RCV002398830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val5819Phe
CA349645132
NM_133432.3:c.17455G>T