Canonical Allele Identifier: PA183682
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179078
ClinVar RCV Id: RCV000155862 RCV000724768 RCV001085039 RCV004019866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe35374Tyr
CA183679
NM_001267550.2:c.106121T>A