Canonical Allele Identifier: PA139008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46703
ClinVar RCV Id: RCV000039973 RCV000205601 RCV000267036 RCV000320876 RCV000325323 RCV000380195 RCV000384525 RCV000770074 RCV001529752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg7545Gln
CA139004
NM_001267550.2:c.22634G>A