Canonical Allele Identifier: PA181629
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178169
ClinVar RCV Id: RCV000154892 RCV000458064 RCV000620291 RCV000725299 RCV001133267 RCV001133263 RCV001133264 RCV001133266 RCV001133265 RCV002467607 RCV003149943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile28331Thr
CA181628
NM_133378.4:c.84992T>C