Canonical Allele Identifier: PA916066597
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165992
ClinVar RCV Id: RCV000152326 RCV000250139 RCV000541819 RCV003137656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala8798Val
CA178776
NM_133437.4:c.26393C>T