Canonical Allele Identifier: PA645409389
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405011
ClinVar RCV Id: RCV000465094 RCV002502610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu9367Phe
CA1999658
NM_001267550.2:c.28099C>T