Canonical Allele Identifier: PA141243
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47517
ClinVar RCV Id: RCV000040786 RCV000249101 RCV000768864 RCV001082069 RCV000714118 RCV001839724 RCV001839725 RCV001839726 RCV001839727 RCV004541192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn28078Ser
CA141241
NM_133378.4:c.84233A>G