Canonical Allele Identifier: PA181643
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96314
ClinVar RCV Id: RCV000082442 RCV000154897 RCV000283095 RCV000298847 RCV000404036 RCV000353742 RCV000246600 RCV000343194 RCV000393180 RCV001080123 RCV001170311 RCV001293236 RCV001270084 RCV004529867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val27228Met
CA181641
NM_133378.4:c.81682G>A