Canonical Allele Identifier: PA2830232630
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165951
ClinVar RCV Id: RCV000152280 RCV000468153 RCV000726091 RCV000852836 RCV001130069 RCV001130070 RCV001130071 RCV001130072 RCV001130073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val10287Leu
CA178665
NM_133437.4:c.30859G>C