Canonical Allele Identifier: PA916065619
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229439
ClinVar RCV Id: RCV000217743 RCV000730718 RCV001079797 RCV001170842 RCV002408935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val6624Phe
CA1995228
NM_133437.4:c.19870G>T