Canonical Allele Identifier: PA309916
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202664
ClinVar RCV Id: RCV000472131 RCV000727759 RCV000769002 RCV001135854 RCV001135855 RCV001135857 RCV001135856 RCV001135858 RCV003235107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16132Cys
CA309914
NM_001267550.2:c.48394C>T