Canonical Allele Identifier: PA282786
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46677
ClinVar RCV Id: RCV000039947 RCV000253741 RCV000291382 RCV000313861 RCV000348985 RCV000400666 RCV000370842 RCV001517444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala6637Val
CA282783
NM_001256850.1:c.19910C>T