Canonical Allele Identifier: PA140796
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_001254479.2:p.Trp25938Ser
CA140792
NM_001267550.2:c.77813G>C