Canonical Allele Identifier: PA112615
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12659
ClinVar RCV Id: RCV000013495 RCV000172493 RCV000219791 RCV000468349 RCV001131435 RCV000769143 RCV000617531 RCV001134416 RCV001134417 RCV001134418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg279Trp
CA256527
NM_001256850.1:c.835C>T