Canonical Allele Identifier: PA302880
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196060
ClinVar RCV Id: RCV000259119 RCV000274523 RCV000299241 RCV000242513 RCV000259353 RCV000317203 RCV000356458 RCV000366970 RCV000487528 RCV001081800 RCV001798632 RCV004528940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg26198Gln
CA302878
NM_001256850.1:c.78593G>A