Canonical Allele Identifier: PA916066074
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405004
ClinVar RCV Id: RCV000475726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala7519Glu
CA1994660
NM_133437.4:c.22556C>A