Canonical Allele Identifier: PA138919
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46671
ClinVar RCV Id: RCV000039941 RCV000172694 RCV001132883 RCV001079880 RCV001132884 RCV001131917 RCV001131918 RCV001131919 RCV001798134 RCV004534864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu5537Lys
CA138917
NM_133378.4:c.16609G>A