Canonical Allele Identifier: PA140794
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47361
ClinVar RCV Id: RCV000040631 RCV000264343 RCV000324153 RCV000389951 RCV000359085 RCV000360289 RCV000476610 RCV000768918 RCV001081320 RCV002336150 RCV004534929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Trp23370Ser
CA140792
NM_133378.4:c.70109G>C