Canonical Allele Identifier: PA2826420691
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518646
ClinVar RCV Id: RCV000619118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val20847Ile
CA349423707
NM_001256850.1:c.62539G>A