Canonical Allele Identifier: PA2830204898
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 425238
ClinVar RCV Id: RCV000488335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile33418Val
CA16621775
NM_133378.4:c.100252A>G