Canonical Allele Identifier: PA302500
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180569
ClinVar RCV Id: RCV000157556 RCV000172379 RCV000222353 RCV000265600 RCV000377872 RCV000322987 RCV000379882 RCV000335757 RCV000476275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Tyr7706Cys
CA302499
NM_133378.4:c.23117A>G