Canonical Allele Identifier: PA178719
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165970
ClinVar RCV Id: RCV000152302 RCV001528481 RCV002433663 RCV000469348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu15868Lys
CA178718
NM_133378.4:c.47602G>A