Canonical Allele Identifier: PA178395
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165682
ClinVar RCV Id: RCV000152170 RCV000727745 RCV001293127 RCV001088064 RCV002371998 RCV003486672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp30254Gly
CA178394
NM_133378.4:c.90761A>G