Canonical Allele Identifier: PA139357
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46848
ClinVar RCV Id: RCV000040118 RCV000172681 RCV001129207 RCV001079188 RCV001170628 RCV001129206 RCV001129208 RCV001129209 RCV001129210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val9223Ile
CA139353
NM_133378.4:c.27667G>A