Canonical Allele Identifier: PA2830208237
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332806
ClinVar RCV Id: RCV000273244 RCV000310901 RCV000325941 RCV000365624 RCV000404582 RCV000643671 RCV002365396 RCV003335308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Trp19236Arg
CA1991706
NM_133378.4:c.57706T>C
CA349434242
NM_133378.4:c.57706T>A