Canonical Allele Identifier: PA138964
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46688
ClinVar RCV Id: RCV000039958 RCV000269064 RCV000384905 RCV000326449 RCV000350254 RCV000388473 RCV000713986 RCV001170080 RCV001086766 RCV004534867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg5979His
CA138962
NM_133378.4:c.17936G>A