Canonical Allele Identifier: PA2830206544
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466889
ClinVar RCV Id: RCV000547280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val5766Ile
CA2001091
NM_133378.4:c.17296G>A