Canonical Allele Identifier: PA645412289
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405190
ClinVar RCV Id: RCV000462005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro32226Thr
CA16610323
NM_001267550.2:c.96676C>A