Canonical Allele Identifier: PA645383730
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332944
ClinVar RCV Id: RCV000301851 RCV000338450 RCV000341719 RCV000396832 RCV000405608 RCV001582975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val2631Ile
CA2004717
NM_133379.5:c.7891G>A