Canonical Allele Identifier: PA283706
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47294
ClinVar RCV Id: RCV000040564 RCV000249890 RCV000227732 RCV000294398 RCV000352767 RCV000295463 RCV000337737 RCV000390725 RCV000768940 RCV001081336 RCV004534924
ClinVar Variation Id: 1740026
ClinVar RCV Id: RCV002332363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala23611Val
CA283702
NM_001267550.2:c.70832C>T
CA2580064879
NM_001267550.2:c.70830_70832delinsTGT