Canonical Allele Identifier: PA645411227
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282019
ClinVar RCV Id: RCV000297529 RCV000301478 RCV000261531 RCV000265016 RCV000304573 RCV000356308 RCV000526427 RCV001798768 RCV002347988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala26961Val
CA1989287
NM_001267550.2:c.80882C>T