Canonical Allele Identifier: PA658664709
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466829
ClinVar RCV Id: RCV000540278 RCV000592077 RCV003330772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr4920Met
CA2002354
NM_001267550.2:c.14759C>T