Canonical Allele Identifier: PA179190
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166291
ClinVar RCV Id: RCV000152476 RCV000286556 RCV000322923 RCV000347185 RCV000377566 RCV000383088 RCV001798485 RCV003137659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val3342Ile
CA179186
NM_133379.5:c.10024G>A