Canonical Allele Identifier: PA181619
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96315
ClinVar RCV Id: RCV000154889 RCV000463812 RCV001727567 RCV004529868 RCV002362733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg28860His
CA181617
NM_133378.4:c.86579G>A