Canonical Allele Identifier: PA2830208082
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467367
ClinVar RCV Id: RCV001130771 RCV001133736 RCV000549166 RCV001133738 RCV000593395 RCV002282219 RCV001130770 RCV001133737 RCV002456151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val18735Met
CA1992002
NM_133378.4:c.56203G>A