Canonical Allele Identifier: PA916066798
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165977
ClinVar RCV Id: RCV000152310 RCV000532070 RCV000852518 RCV001129096 RCV001129098 RCV000730160 RCV001129097 RCV001129099 RCV001129095 RCV004532697 RCV002426723 RCV003486678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val9187Ile
CA178733
NM_133437.4:c.27559G>A