Canonical Allele Identifier: PA645412856
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_001254479.2:p.Gln35354Arg
CA1985167
NM_001267550.2:c.106061A>G