Canonical Allele Identifier: PA140967
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47428
ClinVar RCV Id: RCV000040697 RCV000172229 RCV000283706 RCV000372050 RCV000320147 RCV000341923 RCV000380228 RCV000559104 RCV000620676 RCV000764310 RCV004541183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val27873Ala
CA140964
NM_001267550.2:c.83618T>C