Canonical Allele Identifier: PA140944
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47421
ClinVar RCV Id: RCV000040691 RCV000172628 RCV000252102 RCV001130325 RCV001130327 RCV001130324 RCV001130326 RCV000476606 RCV001130323 RCV001170783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val26083Gly
CA140941
NM_001256850.1:c.78248T>G