Canonical Allele Identifier: PA916065719
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202657
ClinVar RCV Id: RCV000464661 RCV000727858 RCV004525888 RCV002415794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile6966Thr
CA309893
NM_133437.4:c.20897T>C