Canonical Allele Identifier: PA2826428988
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1394301
ClinVar RCV Id: RCV001884767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp33712His
CA1985169
NM_001256850.1:c.101134G>C