Canonical Allele Identifier: PA184462
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179460
ClinVar RCV Id: RCV000156249 RCV000862712 RCV001697085 RCV004544451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Cys11812Arg
CA184461
NM_133378.4:c.35434T>C