Canonical Allele Identifier: PA282800
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46681
ClinVar RCV Id: RCV000039951 RCV000204819 RCV000245217 RCV000261603 RCV000316047 RCV000369529 RCV000319084 RCV000354529 RCV000770083 RCV001082805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp5792Asn
CA282798
NM_133378.4:c.17374G>A