Canonical Allele Identifier: PA141776
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47720
ClinVar RCV Id: RCV000040989 RCV000082477 RCV000241675 RCV001079456 RCV001128833 RCV000986935 RCV001135821 RCV001135822 RCV001171215 RCV001135823 RCV001293191 RCV004537124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met33291Thr
CA141774
NM_133378.4:c.99872T>C