Canonical Allele Identifier: PA2826428989
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238698
ClinVar RCV Id: RCV000232973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln33713Arg
CA1985167
NM_001256850.1:c.101138A>G