Canonical Allele Identifier: PA346744
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180564
ClinVar RCV Id: RCV000157551 RCV000600197 RCV003488406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ala743Thr
CA346741
NM_133379.5:c.2227G>A