Canonical Allele Identifier: PA2826417365
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_001243779.1:p.Ala14751Glu
CA1994660
NM_001256850.1:c.44252C>A