Canonical Allele Identifier: PA141549
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47630
ClinVar RCV Id: RCV000040899 RCV000468674 RCV001133510 RCV001135007 RCV001133509 RCV001133511 RCV001133512 RCV001703915
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu3097Pro
CA141544
NM_133378.4:c.9290T>C