Canonical Allele Identifier: PA178667
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165951
ClinVar RCV Id: RCV000152280 RCV000468153 RCV000726091 RCV000852836 RCV001130069 RCV001130070 RCV001130071 RCV001130072 RCV001130073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val19160Leu
CA178665
NM_001267550.2:c.57478G>C