Canonical Allele Identifier: PA2830236630
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47361
ClinVar RCV Id: RCV000040631 RCV000264343 RCV000324153 RCV000389951 RCV000359085 RCV000360289 RCV000476610 RCV000768918 RCV001081320 RCV002336150 RCV004534929
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Trp17065Ser
CA140792
NM_133437.4:c.51194G>C