Canonical Allele Identifier: PA184056
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179252
ClinVar RCV Id: RCV000156039 RCV001128995 RCV001131670 RCV001131667 RCV001131668 RCV001131669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr5809Pro
CA184055
NM_133378.4:c.17425A>C