Canonical Allele Identifier: PA309735
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202607
ClinVar RCV Id: RCV000184493 RCV000227362 RCV002390477 RCV003137714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile539Asn
CA309733
NM_001256850.1:c.1616T>A