Canonical Allele Identifier: PA141062
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47456
ClinVar RCV Id: RCV000040725 RCV000172219 RCV000291684 RCV000307010 RCV000346476 RCV000402859 RCV000393775 RCV001081280 RCV001170545 RCV002354210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val27254Met
CA141059
NM_001256850.1:c.81760G>A