Canonical Allele Identifier: PA916066664
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413198
ClinVar RCV Id: RCV000595322 RCV001087627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Phe8881Ser
CA1993835
NM_133437.4:c.26642T>C