Canonical Allele Identifier: PA302571
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192086
ClinVar RCV Id: RCV000172479 RCV000260058 RCV000263663 RCV000317593 RCV000321201 RCV000378238 RCV000412681 RCV000553812 RCV003486721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu1359Gly
CA302567
NM_133378.4:c.4076A>G