Canonical Allele Identifier: PA2830191937
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203241
ClinVar RCV Id: RCV000591089 RCV000726948 RCV001087944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro3686Thr
CA311782
NM_133378.4:c.11056C>A