Canonical Allele Identifier: PA181670
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178178
ClinVar RCV Id: RCV000154905 RCV000264981 RCV000389752 RCV000270733 RCV000384089 RCV000329578 RCV000457318 RCV002354368 RCV004534969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met26478Arg
CA181669
NM_133378.4:c.79433T>G