Canonical Allele Identifier: PA140339
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47208
ClinVar RCV Id: RCV000040478 RCV000172649 RCV000244887 RCV001130634 RCV001080680 RCV001170810 RCV001130633 RCV001130635 RCV001129930 RCV001129931 RCV003319176 RCV004541165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg19751Cys
CA140336
NM_001256850.1:c.59251C>T