Canonical Allele Identifier: PA181831
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178222
ClinVar RCV Id: RCV000154957 RCV000531792 RCV001589014 RCV003149947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val10710Ile
CA181830
NM_133378.4:c.32128G>A