Canonical Allele Identifier: PA237708
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191854
ClinVar RCV Id: RCV000172201 RCV000272895 RCV000326514 RCV000286593 RCV000378832 RCV000383680 RCV000610659 RCV000852790 RCV001086287 RCV001798611 RCV002354433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile28102Thr
CA237707
NM_133378.4:c.84305T>C