Canonical Allele Identifier: PA178527
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165854
ClinVar RCV Id: RCV000152226 RCV000230428 RCV000620143 RCV001132547 RCV001133458 RCV001132548 RCV001719940 RCV001132545 RCV001132546 RCV004532692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile21083Ser
CA178526
NM_133378.4:c.63248T>G