Canonical Allele Identifier: PA181735
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178194
ClinVar RCV Id: RCV000154924 RCV000226257 RCV001561005 RCV002326884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu20717Lys
CA181734
NM_133378.4:c.62149G>A