Canonical Allele Identifier: PA2830222478
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448828
ClinVar RCV Id: RCV000517221 RCV000643542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val20476Phe
CA1988182
NM_133432.3:c.61426G>T