Canonical Allele Identifier: PA645409864
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405183
ClinVar RCV Id: RCV000465470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg15197Gly
CA1995414
NM_001267550.2:c.45589A>G