Canonical Allele Identifier: PA645409894
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_001254479.2:p.Val15497Phe
CA1995228
NM_001267550.2:c.46489G>T