Canonical Allele Identifier: PA256532
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12659
ClinVar RCV Id: RCV000013495 RCV000172493 RCV000219791 RCV000468349 RCV001131435 RCV000769143 RCV000617531 RCV001134416 RCV001134417 RCV001134418
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg279Trp
CA256527
NM_133379.5:c.835C>T