Canonical Allele Identifier: PA658659221
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466758
ClinVar RCV Id: RCV000540970 RCV002420448 RCV000592815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val35535Ala
CA1985065
NM_001267550.2:c.106604T>C