Canonical Allele Identifier: PA2830239600
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1386066
ClinVar RCV Id: RCV001905673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Leu21766Val
CA1987532
NM_133437.4:c.65296C>G