Canonical Allele Identifier: PA916067013
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467283
ClinVar RCV Id: RCV000549572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Cys9811Tyr
CA60976860
NM_133437.4:c.29432G>A