Canonical Allele Identifier: PA238058
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191996
ClinVar RCV Id: RCV000172366 RCV000222100 RCV000548036 RCV001132692 RCV001132693 RCV001132694 RCV001132695 RCV001132696 RCV004535175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys10579Gln
CA238057
NM_001267550.2:c.31735A>C