Canonical Allele Identifier: PA178514
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165847
ClinVar RCV Id: RCV000152220 RCV000642992 RCV001133042 RCV001133041 RCV001133043 RCV001311958 RCV001133044 RCV001136490 RCV003486674 RCV002336305 RCV004532691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr21533Asn
CA178513
NM_133378.4:c.64598C>A