Canonical Allele Identifier: PA181840
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178226
ClinVar RCV Id: RCV000154961 RCV000172363 RCV000643341 RCV000770064 RCV001130350 RCV001130352 RCV001135400 RCV001130349 RCV001130351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg9741Trp
CA181838
NM_133378.4:c.29221C>T